Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177331G= , CM000678.2:g.177331G= | GRCh38 |
| NC_000016.9:g.227330G= , CM000678.1:g.227330G= | GRCh37 |
| NC_000016.8:g.167330G= | NCBI36 |
| NG_000006.1:g.38194G= | |
| NG_059186.1:g.5681G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.349G= MANE Select | ENSP00000322421.5:p.Glu117= | |
| ENST00000397797.1:c.253G= | ENSP00000380899.1:p.Glu85= | |
| ENST00000472694.1:n.485G= | ||
| NM_000558.4:c.349G= | NP_000549.1:p.Glu117= | |
| NM_000558.5:c.349G= MANE Select | NP_000549.1:p.Glu117= |